Project Manager (Engineering)

Primary Talent Partners, LLC; Lafayette (CO); Presencial; USD 83.000 - 96.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Supplemental benefits package

Descripción de la vacante

Primary Talent Partners is seeking a Project Manager (Engineering) for a 14-month contract in Lafayette, CO. You will lead MDR implementation and compliance change-control projects across Regulatory Affairs, Quality, Engineering, and Manufacturing to ensure released products meet EU MDR and provide ongoing supply continuity.

The role requires a Bachelor's degree and 7+ years of relevant experience (or an advanced degree with 5+ years) and experience coordinating cross-functional teams, managing

Formación

• Bachelor's degree and a minimum of 7 years of relevant experience, or an advanced degree with a minimum of 5 years.
• Demonstrated experience leading complex cross-functional projects in medical devices or regulated products.
• Strong ability to translate regulatory, quality, and technical requirements into executable plans.
• Experience coordinating with OEMs, contract manufacturers, or external suppliers.
• Experience managing schedules, budgets, risks, governance, and executive communications.

Responsabilidades

• Lead MDR implementation and compliance change-control projects for released products from initiation to closure.
• Guide cross-functional teams to align execution with compliance and business objectives.
• Develop integrated plans linking technical deliverables with regulatory and quality requirements.
• Coordinate MDR transition planning with OEMs and suppliers.
• Manage scope, schedules, budgets, risks, and governance; provide data-driven updates to leadership.

Conocimientos

PMP

Lean

Six Sigma

Stakeholder mgmt

Regulatory compliance

Educación

Bachelor's degree

Advanced degree

Descripción del empleo

Primary Talent Partners has a new contract opening for a Project Manager (Engineering) with our medical device client in Lafayette, CO. This is a 14-month contract with a potential for extension. Pay: $60.00 - $70.00/hr;W2 contract, no PTO, no Benefits. ACA-compliant supplemental package available for enrollment.Candidates must be legally authorized to work in the United States and must be able to sit on Primary Talent Partners W2 without sponsorship.

Schedule: Day Shift - M-F, 9am-5pm

Description: Careers that Change Lives
As a Principal Project Management Specialist within the Compliance PMO, you will lead complex EU Medical Device Regulation (MDR) implementation and compliance change-control projects for released products. You will align Regulatory Affairs, Quality, Engineering, Operations, Supply Chain, manufacturing sites, original equipment manufacturers (OEMs), contract manufacturers, and external suppliers to translate compliance requirements into executable plans.

Your work will protect compliant product availability and continuity of supply while strengthening released-product implementation, operational readiness, risk management, and change execution. This role is ideal for an experienced project leader who combines disciplined program management, operational judgment, and influence across internal and external organizations.

A Day in the Life:

• Lead multiple complex MDR implementation and compliance change-control projects for released products from project initiation through closure.
• Guide cross-functional teams across Regulatory Affairs, Quality, Engineering, Manufacturing, Operations, Supply Chain Planning, Supplier Quality, and other partners to align execution with compliance and business objectives.
• Develop integrated plans connecting technical deliverables, regulatory and quality requirements, supplier activities, operational constraints
• Collaborate with OEMs for MDR Transition planning by establishing deliverables, milestones, decision rights, escalation paths, recovery actions, and readiness expectations.
• Coordinate released-product changes across components, suppliers, manufacturing processes, specifications, packaging, labeling, quality systems, and regulatory requirements.
• Manage scope, schedules, budgets, resources, risks, assumptions, dependencies, decisions, governance, and reporting; use operational data to identify constraints and elevate issues with clear options and recommendations.
• Lead meetings and readiness reviews, maintain decisions and action ownership, and communicate concise updates to teams, leaders, sites, and external partners.
• Advance portfolio priorities and PMO practices through lessons learned, data-driven insights, coaching, and influence without direct authority.
• This position is located in Lafayette, CO. Travel up to 25%, primarily in US.

Qualifications - To thrive in this role, you must have:

• Bachelor's degree and a minimum of 7 years of relevant experience, or an advanced degree with a minimum of 5 years. Degrees earned outside the United States must meet applicable equivalency requirements.
• Demonstrated experience leading complex, interdependent cross-functional projects or programs in medical devices, regulated products, manufacturing, operations, supply chain, product lifecycle management, or a comparable environment.
• Strong operational knowledge of released or commercialized products, including translating technical, quality, regulatory, supply, and business requirements into executable plans.
• Direct experience leading complex technical or operational work with OEMs, contract manufacturers, or external suppliers.
• Experience managing integrated schedules, budgets, risks, dependencies, governance, executive communications, and cross-functional decisions.
• Ability to influence, establish accountability, negotiate, resolve conflict, and communicate complex information across teams, leaders, executives, and external organizations without direct authority.
• Ability to work independently through ambiguity, changing priorities, resource constraints, and issues requiring structured investigation and practical problem solving.

Nice to Have:

• Experience with EU MDR implementation, regulatory remediation, compliance programs, or global released-product lifecycle management.
• Experience leading supplier transitions, manufacturing or process changes, capacity or continuity initiatives, component obsolescence, quality improvement, remediation, or cost-improvement programs for commercialized products.
• Working knowledge of medical-device quality systems, design and change controls, validation, risk and configuration management, and applicable regulatory standards.
• Degree in Engineering, Operations, Supply Chain, a scientific discipline, or equivalent industry experience; an advanced technical degree or MBA is preferred.
• PMP, Lean, Six Sigma, or comparable project-management or operational-excellence certification.
• Business acumen and experience using AI-powered tools to improve analysis, productivity, communication, decisions, or business outcomes

Primary Talent Partners is an Equal Opportunity / Affirmative Action employer committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, national origin, disability, protected veteran status, gender identity, or any other factor protected by applicable federal, state, or local laws.

If you are a person with a disability needing assistance with the application or at any point in the hiring process, please contact us at [e-mail]

#PTPJobs